Canonical Allele Identifier: PA2573066361
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 1333671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Ser1633Tyr
CA353352200
NM_001164317.2:c.4898C>A